Fusion formable alkali-free intermediate thermal expansion coefficient glass

ABSTRACT

A compositional range of high strain point and/or intermediate expansion coefficient alkali metal free aluminosilicate and boroaluminosilicate glasses are described herein. The glasses can be used as substrates or superstrates for photovoltaic devices, for example, thin film photovoltaic devices such as CdTe or CIGS photovoltaic devices or crystalline silicon wafer devices. These glasses can be characterized as having strain points ≧600° C., thermal expansion coefficient of from 35 to 50×10 −7 /° C.

This application is a continuation Application of U.S. patentapplication Ser. No. 13/569,756 filed on Aug. 8, 2012 which claims thebenefit of priority under 35 U.S.C. §119 of U.S. Provisional ApplicationSer. No. 61/522,956 filed on Aug. 12, 2011 the entire disclosure of eachis relied upon and incorporated herein by reference in their entirety.

BACKGROUND

Field

Embodiments relate generally to alkali-free glasses and moreparticularly to alkali-free, high strain point and/or intermediateexpansion coefficient, fusion formable aluminosilicate, and/orboroaluminosilicate glasses which may be useful in photovoltaicapplications, for example, thin film photovoltaic devices.

Technical Background

Substrate glasses for copper indium gallium diselenide (CIGS)photovoltaic modules typically contain Na₂O, as diffusion of Na from theglass into the CIGS layer has been shown to result in significantimprovement in module efficiency. However, due to the difficulty incontrolling the amount of diffusing Na during the CIGSdeposition/crystallization process, some manufacturers of these devicesprefer to deposit a layer of a suitable Na compound, e.g. NaF, prior toCIGS deposition, in which case any alkali present in the substrate glassneeds to be contained through the use of a barrier layer. Moreover, inthe case of cadmium telluride (CdTe) photovoltaic modules, any Nacontamination of the CdTe layer is deleterious to module efficiency and,therefore, typical Na-containing substrate glasses, e.g. soda-limeglass, require the presence of a barrier layer. Consequently, use of analkali-free substrate glass for either CIGS, silicon, waferedcrystalline silicon, or CdTe modules can obviate the need for a barrierlayer.

SUMMARY

The intermediate thermal expansion coefficient and/or the alkali-freeglasses disclosed herein are especially compatible with CdTephotovoltaic devices and may increase the efficiency of the cell.

One embodiment is a glass comprising, in mole percent:

-   -   55 to 75 percent SiO₂;    -   5 to 20 percent Al₂O₃;    -   0 to 15 percent B₂O₃;    -   0 to 10 percent MgO;    -   0 to 15 percent SrO;    -   0 to 16 percent CaO; and    -   0 to 9 percent BaO.        wherein MgO+CaO+BaO+SrO is 13 to 20 percent, wherein the glass        is substantially free of alkali metal, and wherein the glass has        a liquidus viscosity of 100,000 poise or greater.

These glasses are advantageous materials to be used in copper indiumgallium diselenide (CIGS) photovoltaic modules where the sodium requiredto optimize cell efficiency is not to be derived from the substrateglass but instead from a separate deposited layer consisting of a sodiumcontaining material such as NaF. Current CIGS module substrates aretypically made from soda-lime glass sheet that has been manufactured bythe float process. However, use of higher strain point glass substratescan enable higher temperature CIGS processing, which is expected totranslate into desirable improvements in cell efficiency.

Accordingly, the alkali-free glasses described herein can becharacterized by strain points ≧600° C. and thermal expansioncoefficients in the range of from 35 to 50×10⁻⁷/° C., in order tominimize thermal expansion mismatch between the substrate and CIGS layeror to better match the thermal expansion of CdTe.

Finally, the preferred compositions of this disclosure have strain pointwell in excess of 650° C., thereby enabling CIGS or CdTedeposition/crystallization to be carried out at the highest possibleprocessing temperature, resulting in additional efficiency gain.

Additional features and advantages will be set forth in the detaileddescription which follows, and in part will be readily apparent to thoseskilled in the art from the description or recognized by practicing theinvention as described in the written description and claims hereof.

It is to be understood that both the foregoing general description andthe following detailed description are merely exemplary of theinvention, and are intended to provide an overview or framework forunderstanding the nature and character of the invention as it isclaimed.

The accompanying drawing is included to provide a further understandingof the invention, and is incorporated in and constitutes a part of thisspecification. The drawing illustrates one or more embodiment(s) of theinvention and together with the description serve to explain theprinciples and operation of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention can be understood from the following detailed descriptioneither alone or together with the accompanying drawing FIGURE.

The FIGURE is a schematic of features of a photovoltaic device accordingto some embodiments.

DETAILED DESCRIPTION

Reference will now be made in detail to various embodiments of theinvention.

As used herein, the term “substrate” can be used to describe either asubstrate or a superstrate depending on the configuration of thephotovoltaic cell. For example, the substrate is a superstrate, if whenassembled into a photovoltaic cell, it is on the light incident side ofa photovoltaic cell. The superstrate can provide protection for thephotovoltaic materials from impact and environmental degradation whileallowing transmission of the appropriate wavelengths of the solarspectrum. Further, multiple photovoltaic cells can be arranged into aphotovoltaic module. Photovoltaic device can describe either a cell, amodule, or both.

As used herein, the term “adjacent” can be defined as being in closeproximity. Adjacent structures may or may not be in physical contactwith each other. Adjacent structures can have other layers and/orstructures disposed between them.

Moreover, where a range of numerical values is recited herein,comprising upper and lower values, unless otherwise stated in specificcircumstances, the range is intended to include the endpoints thereof,and all integers and fractions within the range. It is not intended thatthe scope of the invention be limited to the specific values recitedwhen defining a range. Further, when an amount, concentration, or othervalue or parameter is given as a range, one or more preferred ranges ora list of upper preferable values and lower preferable values, this isto be understood as specifically disclosing all ranges formed from anypair of any upper range limit or preferred value and any lower rangelimit or preferred value, regardless of whether such pairs areseparately disclosed. Finally, when the term “about” is used indescribing a value or an end-point of a range, the disclosure should beunderstood to include the specific value or end-point referred to.

As used herein, the term “about” means that amounts, sizes,formulations, parameters, and other quantities and characteristics arenot and need not be exact, but may be approximate and/or larger orsmaller, as desired, reflecting tolerances, conversion factors, roundingoff, measurement error and the like, and other factors known to those ofskill in the art. In general, an amount, size, formulation, parameter orother quantity or characteristic is “about” or “approximate” whether ornot expressly stated to be such.

The term “or”, as used herein, is inclusive; more specifically, thephrase “A or B” means “A, B, or both A and B”. Exclusive “or” isdesignated herein by terms such as “either A or B” and “one of A or B”,for example.

The indefinite articles “a” and “an” are employed to describe elementsand components of the invention. The use of these articles means thatone or at least one of these elements or components is present. Althoughthese articles are conventionally employed to signify that the modifiednoun is a singular noun, as used herein the articles “a” and “an” alsoinclude the plural, unless otherwise stated in specific instances.Similarly, the definite article “the”, as used herein, also signifiesthat the modified noun may be singular or plural, again unless otherwisestated in specific instances.

It is noted that one or more of the claims may utilize the term“wherein” as a transitional phrase. For the purposes of defining thepresent invention, it is noted that this term is introduced in theclaims as an open-ended transitional phrase that is used to introduce arecitation of a series of characteristics of the structure and should beinterpreted in like manner as the more commonly used open-ended preambleterm “comprising.”

As used herein, a glass composition having 0 wt % of a compound isdefined as meaning that the compound, molecule, or element was notpurposefully added to the composition, but the composition may stillcomprise the compound, typically in tramp or trace amounts. Similarly,“substantially free of alkali metal”, “substantially free of sodium”,“substantially free of potassium”, “sodium-free,” “alkali-free,”“potassium-free” or the like are defined to mean that the compound,molecule, or element was not purposefully added to the composition, butthe composition may still comprise sodium, alkali, or potassium, but inapproximately tramp or trace amounts. These tramp amounts are notintentionally included in the batch but may be present in minor amountsas impurities in the raw materials used to provide the major componentsof the glass.

One embodiment is a glass comprising, in mole percent:

-   -   55 to 75 percent SiO₂;    -   5 to 20 percent Al₂O₃;    -   0 to 15 percent B₂O₃;    -   0 to 10 percent MgO;    -   0 to 15 percent SrO;    -   0 to 16 percent CaO; and    -   0 to 9 percent BaO.        wherein MgO+CaO+BaO+SrO is 13 to 20 percent, wherein the glass        is substantially free of alkali metal, and wherein the glass has        a liquidus viscosity of 100,000 poise or greater.

In one embodiment, the glass, comprises, in mole percent:

-   -   55 to 75 percent SiO₂;    -   5 to 13 percent Al₂O₃;    -   0 to 15 percent B₂O₃;    -   0 to 10 percent MgO;    -   0 to 15 percent SrO;    -   0 to 16 percent CaO; and    -   0 to 9 percent BaO.

In one embodiment, the glass, comprises, in mole percent:

-   -   55 to 75 percent SiO₂;    -   0 to 20 percent Al₂O₃;    -   6 to 12 percent B₂O₃;    -   0 to 10 percent MgO;    -   0 to 15 percent SrO;    -   0 to 16 percent CaO; and    -   0 to 9 percent BaO.

In one embodiment, the glass, comprises, in mole percent:

-   -   55 to 75 percent SiO₂;    -   5 to 13 percent Al₂O₃;    -   6 to 12 percent B₂O₃;    -   0 to 10 percent MgO;    -   0 to 15 percent SrO;    -   0 to 16 percent CaO; and    -   0 to 9 percent BaO.

In one embodiment, the glass, comprises, in mole percent:

-   -   55 to 75 percent SiO₂;    -   8 to 13 percent Al₂O₃;    -   6 to 12 percent B₂O₃;    -   0 to 7 percent MgO;    -   0 to 12 percent SrO;    -   0 to 16 percent CaO; and    -   0 to 9 percent BaO.

In one embodiment, the glass, comprises, in mole percent:

-   -   58 to 69 percent SiO₂;    -   8 to 13 percent Al₂O₃;    -   6 to 12 percent B₂O₃;    -   0 to 7 percent MgO;    -   0 to 12 percent SrO;    -   0 to 16 percent CaO; and    -   0 to 9 percent BaO.

In one embodiment, the glass, comprises, in mole percent:

-   -   73 to 75 percent SiO₂;    -   6 to 9 percent Al₂O₃;    -   0 percent B₂O₃;    -   1 to 3 percent MgO;    -   0 percent SrO;    -   13 to 16 percent CaO; and    -   1 to 3 percent BaO.

In one embodiment, the glass, comprises, in mole percent:

-   -   60 to 67 percent SiO₂;    -   8 to 12 percent Al₂O₃;    -   6 to 12 percent B₂O₃;    -   0.05 to 7 percent MgO;    -   0 to 12 percent SrO;    -   0.5 to 9 percent CaO; and    -   0.5 to 8 percent BaO.

The glass is substantially free of alkali metal, for example, thecontent of alkali can be 0.05 mole percent or less, for example, zeromole percent. The glass, according to some embodiments, is free ofintentionally added alkali metal.

The glass is substantially free of sodium, for example, the content ofsodium can be 0.05 mole percent or less, for example, zero mole percent.The glass, according to some embodiments, is free of intentionally addedsodium.

The glass is substantially free of potassium, for example, the contentof sodium can be 0.05 mole percent or less, for example, zero molepercent. The glass, according to some embodiments, is free ofintentionally added potassium.

The glass is substantially free of sodium and potassium, for example,the content of sodium can be 0.05 mole percent or less, for example,zero mole percent. The glass, according to some embodiments, is free ofintentionally added sodium and potassium.

In some embodiments, the glass comprises 55 to 75 percent SiO₂, forexample, 58 to 69 percent SiO₂, or, for example, 60 to 67 percent SiO₂,or, for example, 73 to 75 percent SiO₂.

As mentioned above, the glasses, according some embodiments, comprise 0to 15 percent B₂O₃, for example, 6 to 12 percent. B₂O₃ is added to theglass to reduce melting temperature, to decrease liquidus temperature,to increase liquidus viscosity, and to improve mechanical durabilityrelative to a glass containing no B₂O₃.

The glass, according to some embodiments, comprises MgO+CaO+BaO+SrO inan amount from 13 to 20 mole percent. MgO can be added to the glass toreduce melting temperature and to increase strain point. It candisadvantageously lower CTE relative to other alkaline earths (e.g.,CaO, SrO, BaO), and so other adjustments may be made to keep the CTEwithin the desired range. Examples of suitable adjustments includeincrease SrO at the expense of CaO.

The glasses can comprise, in some embodiments, 0 to 15 mole percent SrO,for example, greater than zero to 15 mole percent, for example, 1 to 12mole percent SrO. In certain embodiments, the glass contains nodeliberately batched SrO, though it may of course be present as acontaminant in other batch materials. SrO contributes to highercoefficient of thermal expansion, and the relative proportion of SrO andCaO can be manipulated to improve liquidus temperature, and thusliquidus viscosity. SrO is not as effective as CaO or MgO for improvingstrain point, and replacing either of these with SrO tends to cause themelting temperature to increase. BaO has a similar effect coefficient ofthermal expansion as SrO, if not a greater effect. BaO tends to lowermelting temperature and lower liquidus temperature

The glasses, in some embodiments, comprise 0 to 16 mole percent CaO, forexample, greater than 0 to 15 or, for example, 0 to 12 mole percent CaO,for example, 0.5 to 9 mole percent CaO. CaO contributes to higher strainpoint, lower density, and lower melting temperature.

The glass, according to one embodiment, further comprises 0 to 0.5 molepercent of a fining agent. The fining agent can be SnO₂.

The glass, according to one embodiment, further comprising 0 to 2 molepercent of TiO₂, MnO, ZnO, Nb₂O₅, Ta₂O₅, ZrO₂, La₂O₃, Y₂O₃, P₂O₅, or acombination thereof. These optional components can be used to furthertailor glass properties.

In some embodiments, the glass is substantially free of Sb₂O₃, As₂O₃, orcombinations thereof, for example, the glass comprises 0.05 mole percentor less of Sb₂O₃ or As₂O₃ or a combination thereof. For example, theglass can comprise zero mole percent of Sb₂O₃ or As₂O₃ or a combinationthereof.

Accordingly, in one embodiment, the glass has a strain point of 600° C.or greater, for example, 610° C. or greater, for example, 620° C. orgreater, for example, 630° C. or greater, for example, 640° C. orgreater, for example, 650° C. or greater. In some embodiments, the glasshas a coefficient of thermal expansion of from 35×10⁻⁷/° C. to 50×10⁻⁷/°C., for example, 39×10⁻⁷/° C. to 50×10⁻⁷/° C. In one embodiment, theglass has a coefficient of thermal expansion of from 35×10⁻⁷/° C. to50×10⁻⁷/° C. and a strain point of 600° C. or greater.

The glass can be fusion formed as known in the art of fusion formingglass. The fusion draw process uses an isopipe that has a channel foraccepting molten glass raw material. The channel has weirs that are openat the top along the length of the channel on both sides of the channel.When the channel fills with molten material, the molten glass overflowsthe weirs. Due to gravity, the molten glass flows down the outsidesurfaces of the isopipe. These outside surfaces extend down and inwardlyso that they join at an edge below the drawing tank. The two flowingglass surfaces join at this edge to fuse and form a single flowingsheet. The fusion draw method offers the advantage that, since the twoglass films flowing over the channel fuse together, neither outsidesurface of the resulting glass sheet comes in contact with any part ofthe apparatus. Thus, the surface properties are not affected by suchcontact.

Glasses having a liquidus viscosity of greater than or equal to 100 kP,100,000 poise, are usually fusion formable. Glass having a liquidusviscosity in the range of from 10 kP to less than 100 kP are usuallyfloat formable but not fusion formable. Some embodiments are alkali-freeglasses with Tstr>630° C., α in the range of 4-5 ppm/° C., as well asliquidus viscosity (ηliq) in excess of 100,000 poise. As such, they areideally suited for being formed into sheet by the fusion process.Moreover, many of these glasses also have a 200 poise temperature (T₂₀₀)that is well below 1550° C., making them ideal candidates for lower-costversions of the fusion process.

In one embodiment, the glass is in the form of a sheet. The glass in theform of a sheet can be strengthened, for example, thermally tempered.

The glass, according to one embodiment, is optically transparent.

In one embodiment, as shown in the FIGURE, a photovoltaic device 100comprises the glass in the form of a sheet 10. The photovoltaic devicecan comprise more than one of the glass sheets, for example, as asubstrate and/or as a superstrate. In one embodiment, the photovoltaicdevice 100 comprises the glass sheet as a substrate or superstrate 10 or18, a conductive material 12 adjacent to the substrate, and an activephotovoltaic medium 16 adjacent to the conductive material. In oneembodiment, the device comprises two glass sheets, one as thesuperstrate and one as the substrate, having the compositions describedherein. The functional layer can comprise copper indium galliumdiselenide, amorphous silicon, crystalline silicon, one or morecrystalline silicon wafers, cadmium telluride, or combinations thereofadjacent to the substrate or superstrate. In one embodiment, the activephotovoltaic medium comprises a CIGS layer. In one embodiment, theactive photovoltaic medium comprises a cadmium telluride (CdTe) layer.In one embodiment, the photovoltaic device comprises a functional layercomprising copper indium gallium diselenide or cadmium telluride. In oneembodiment, the photovoltaic device the functional layer is copperindium gallium diselenide. In one embodiment, the functional layer iscadmium telluride.

The photovoltaic device 100, according to one embodiment, furthercomprises one or more intermediate layer(s) 14 such as a sodiumcontaining layer, for example, a layer comprising NaF or a barrier layerdisposed between or adjacent to the superstrate or substrate and thefunctional layer. In one embodiment, the photovoltaic device furthercomprises a barrier layer disposed between or adjacent to thesuperstrate or substrate and a transparent conductive oxide (TCO) layer,wherein the TCO layer is disposed between or adjacent to the functionallayer and the barrier layer. A TCO may be present in a photovoltaicdevice comprising a CdTe functional layer. In one embodiment, thebarrier layer is disposed directly on the glass. In one embodiment, thedevice comprises multiple intermediate layers such as a sodiumcontaining layer, for example, a layer comprising NaF, and an adjacentsodium metering layer located between the superstrate and the substrate.

In one embodiment, the glass sheet is optically transparent. In oneembodiment, the glass sheet as the substrate and/or superstrate isoptically transparent.

According to some embodiments, the glass sheet has a thickness of 4.0 mmor less, for example, 3.5 mm or less, for example, 3.2 mm or less, forexample, 3.0 mm or less, for example, 2.5 mm or less, for example, 2.0mm or less, for example, 1.9 mm or less, for example, 1.8 mm or less,for example, 1.5 mm or less, for example, 1.1 mm or less, for example,0.5 mm to 2.0 mm, for example, 0.5 mm to 1.1 mm, for example, 0.7 mm to1.1 mm. Although these are exemplary thicknesses, the glass sheet canhave a thickness of any numerical value including decimal places in therange of from 0.1 mm up to and including 4.0 mm.

Alkali-free glasses are becoming increasingly attractive candidates forthe superstrate, substrate of CdTe, CIGS modules, respectively. In theformer case, alkali contamination of the CdTe and conductive oxidelayers of the film stack is avoided. Moreover, process simplificationarises from the elimination of the barrier layer (needed, e.g., in thecase of conventional soda-lime glass). In the latter case, CIGS modulemanufacturers are better able to control the amount of Na needed tooptimize absorber performance by depositing a separate Na-containinglayer that, by virtue of its specified composition and thickness,results in more reproducible Na delivery to the CIGS layer.

EXAMPLES

Table 1, Table 2, Table 3, Table 4, Table 5, Table 6, and Table 7 showexemplary glasses, according to embodiments of the invention. Propertiesdata for some exemplary glasses are also shown in Table 1, Table 2,Table 3, Table 4, Table 5, Table 6, and Table 7. In the Tables T_(str)(°C.) is the strain point which is the temperature when the viscosity isequal to 10^(14.7) P as measured by beam bending or fiber elongation.α(10⁻⁷/° C.) in the Tables is the coefficient of thermal expansion (CTE)which is the amount of dimensional change from either 0 to 300° C. or 25to 300° C. depending on the measurement. CTE is typically measured bydilatometry. ρ(g/cc) is the density which is measured with theArchimedes method (ASTM C693). T₂₀₀(° C.) is the two-hundred Poise (P)temperature. This is the temperature when the viscosity of the melt is200P as measured by HTV (high temperature viscosity) measurement whichuses concentric cylinder viscometry. T_(liq)(° C.) is the liquidustemperature. This is the temperature where the first crystal is observedin a standard gradient boat liquidus measurement (ASTM C829-81). ρ_(liq)is the liquidus viscosity expressed in kilopoise; thus 100 kP=100,000 P.This is the viscosity of the melt corresponding to the liquidustemperature.

TABLE 1 Example Mole % 1 2 3 4 5 6 7 8 9 10 MgO 6.4 6.9 6.9 4.6 4.8 6.44.4 4.4 2.7 2.6 CaO 8.5 6.9 9.1 5.4 5.6 5.2 7.2 5.2 2.9 2.0 SrO 0 0 03.6 3.8 3.5 3.5 5.5 11.8 9.6 BaO 2.4 3.4 2.6 2.4 2.5 2.3 2.3 2.3 0.7 3.6RO 17.2 17.2 18.6 16.0 16.7 17.4 17.4 17.4 18.0 17.7 B₂O₃ 10.0 10.0 10.810.7 11.2 10.3 10.3 10.3 9.0 7.5 Al₂O₃ 11.1 11.1 12.0 11.1 11.6 10.710.7 10.7 9.6 9.3 SiO₂ 61.5 61.5 58.5 62.0 60.5 61.5 61.5 61.5 63.3 65.4SnO₂ 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10 Tstr 645 642 641643 641 642 641 642 645 649 α 41.8 40.6 41.5 40.7 41.2 40.0 41.0 41.946.2 46.5 ρ 2.53 2.56 2.56 2.57 2.59 2.58 2.58 2.62 2.70 2.75 T200 14731490 1515 Tliq 1060 1065 1050 1015 1020 1070 1040 1035 1130 1110 ηliq205 777 459 (kP)

TABLE 2 Example Mole % 11 12 13 14 15 16 17 18 19 20 MgO 4.1 5.4 1.8 02.0 4.4 6.4 5.4 5.4 6.4 CaO 9.9 6.4 11.0 10.0 9.0 8.5 6.5 7.5 7.5 7.5SrO 3.3 4.3 2.9 9.0 8.0 2.0 2.0 1.0 1.0 0 BaO 2.2 2.8 3.3 0 0 2.4 2.43.4 3.4 3.4 RO 19.4 19.0 19.0 19.0 19.0 17.3 17.3 17.3 17.3 17.3 B₂O₃9.7 10.7 10.7 8.0 8.0 10.0 10.0 10.0 9.0 9.0 Al₂O₃ 10.0 11.1 8.5 9.0 9.011.1 11.1 11.1 12.1 12.1 SiO₂ 60.8 59.0 62.3 64.0 64.0 61.5 61.5 61.561.5 61.5 SnO₂ 0.10 0.10 0.07 0.10 0.10 0.10 0.10 0.10 0.10 0.10 Tstr639 636 631 648 649 650 645 650 659 661 α 46.5 43.9 46.0 48.4 45.8 40.441.4 39.5 40.3 39.8 ρ 2.70 2.64 2.67 2.63 2.57 2.60 2.56 2.60 2.58 T2001423 Tliq 1045 1030 1075 1150 1145 1080 1080 1095 1080 1090 ηliq 192(kP)

TABLE 3 Example Mole % 21 22 23 24 25 26 27 28 29 30 MgO 0.1 2.0 0 01.98 1.97 0.07 0.07 0.06 0.06 CaO 4.3 2.0 4.3 3.3 1.3 0.8 4.6 4.6 4.54.6 SrO 9.7 12.0 10.0 10.5 11.9 11.5 9.7 9.6 10.2 9.5 BaO 0.1 0.1 0.10.1 2.0 4.0 0.1 0.1 0.1 0.1 RO 14.1 16.1 14.4 13.9 17.2 18.3 14.4 14.414.8 14.2 B₂O₃ 8.4 6.6 8.5 8.5 6.4 6.4 9.9 11.4 9.9 11.5 Al₂O₃ 9.3 9.310.0 10.5 8.7 8.6 9.3 9.3 10.0 10.0 SiO₂ 68.1 67.8 67.0 67.0 67.6 66.566.2 64.8 65.2 64.1 SnO₂ 0.16 0.18 0.18 0.18 0.17 0.17 0.17 0.17 0.170.17 Tstr 668 674 668 673 667 665 658 649 659 656 α 40.9 42.8 41.7 41.845.9 46.6 42.1 42.5 42.3 42.4 ρ 2.59 2.65 2.59 2.59 2.72 2.77 2.58 2.582.59 2.59 T200 1595 1595 1594 1610 1563 1545 1569 1540 1555 1528 Tliq1125 1125 1135 1150 1100 1075 1075 1070 1080 1080 ηliq 142 162 119 121124 235 274 202 253 163 (kP)

TABLE 4 Example Mole % 31 32 33 34 35 36 37 38 MgO 4.7 2.5 3.5 4.5 3.83.9 4.2 4.4 CaO 5.6 7.0 5.5 4.5 6.0 5.7 5.6 5.5 SrO 3.7 1.5 2.0 2.0 2.22.5 2.9 3.3 BaO 2.5 7.0 7.0 7.0 7.6 6.2 4.9 3.7 RO 16.5 18.0 18.0 18.019.5 18.3 17.6 16.8 B₂O₃ 11.0 9.0 9.0 9.0 9.8 9.8 10.1 10.4 Al₂O₃ 11.49.0 9.0 9.0 9.8 9.9 10.3 10.8 SiO₂ 61.0 63.9 63.9 63.9 60.9 62.0 62.062.0 SnO₂ 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10 Tstr 640 632 632 635630 631 633 638 α 41.2 46.5 45.9 45.8 48.2 46.0 43.7 41.7 ρ 2.58 2.732.72 2.72 2.77 2.71 2.67 2.62 T200 1510 1490 1490 1494 1443 1475 1490Tliq 1000 1050 1025 1020 1045 1000 1010 ηliq (kP) 893 166 364 437 106756 808

TABLE 5 Example Mole % 39 40 41 42 43 44 45 46 47 48 MgO 1.4 1.3 1.8 0.02.0 4.4 6.4 5.4 5.4 6.4 CaO 15.4 14.2 11.0 10.0 9.0 8.5 6.5 7.5 7.5 7.5SrO 2.9 9.0 8.0 2.0 2.0 1.0 1.0 0 BaO 1.4 1.3 3.3 0 0 2.4 2.4 3.4 3.43.4 RO 18.1 16.7 19.0 19.0 19.0 17.3 17.3 17.3 17.3 17.3 B₂O₃ 10.7 8.08.0 10.0 10.0 10.0 9.0 9.0 Al₂O₃ 7.0 8.4 8.5 9.0 9.0 11.1 11.1 11.1 12.112.1 SiO₂ 74.9 74.9 62.3 64.0 64.0 61.5 61.5 61.5 61.5 61.5 SnO₂ 0.100.10 0.07 0.10 0.10 0.10 0.10 0.10 0.10 0.10 Tstr 735 745 613 648 649650 645 650 659 661 α 42.7 40.6 46 48.4 45.8 40.4 41.4 39.5 40.3 39.8 ρ2.67 2.67 2.63 2.57 2.60 2.56 2.60 2.58 T200 Tliq 1080 1080 1075 11501145 1080 1080 1095 1080 1090 ηliq (kP)

TABLE 6 Example Mole % 49 50 51 52 53 54 55 56 57 MgO 0.1 2.0 0.0 0.02.0 2.0 0.1 0.1 0.1 CaO 4.3 2.0 4.3 3.3 1.3 0.8 4.6 4.6 4.5 SrO 9.7 12.010.0 10.5 11.9 11.5 9.7 9.6 10.2 BaO 0.1 0.1 0.1 0.1 2.0 4.0 0.1 0.1 0.1RO 14.1 16.1 14.4 13.9 17.2 18.3 14.4 14.4 14.8 B₂O₃ 8.4 6.6 8.5 8.5 6.46.4 9.9 11.4 9.9 Al₂O₃ 9.3 9.3 10.0 10.5 8.6 8.6 9.3 9.3 9.9 SiO₂ 68.167.8 67.0 66.9 67.6 66.5 66.2 64.8 65.2 SnO₂ 0.16 0.18 0.18 0.18 0.170.17 0.17 0.17 0.17 Tstr 668 674 668 673 667 665 658 649 659 α 40.9 42.841.7 41.8 45.9 46.6 42.1 42.5 42.3 ρ 2.59 2.65 2.59 2.59 2.72 2.77 2.582.58 2.59 T200 1595 1595 1594 1610 1563 1545 1569 1540 1555 Tliq 11251125 1135 1150 1100 1075 1075 1070 1080 ηliq (kP) 142 162 119 121 124235 274 202 253

TABLE 7 Example Mole % 58 59 60 61 62 MgO 0.1 0.1 1.6 0.1 0.1 CaO 4.65.0 4.9 6.5 8.0 SrO 9.5 9.8 8.4 8.5 6.9 BaO 0.1 0.1 0.1 0.1 0.1 RO 14.215.0 15.0 15.1 15.1 B₂O₃ 11.5 10.4 10.3 10.3 10.4 Al₂O₃ 10.0 9.7 9.6 9.69.6 SiO₂ 64.1 64.9 65.0 64.8 64.8 SnO₂ 0.17 0.16 0.16 0.16 0.16 Tstr 656655 653 657 656 α 42.4 42 41.8 42 42.5 ρ 2.59 2.60 2.56 2.57 2.55 T2001528 1539 1546 1539 1536 Tliq 1080 1090 1100 1100 1080 ηliq (kP) 163 132136 106 178

It will be apparent to those skilled in the art that variousmodifications and variations can be made to the present inventionwithout departing from the spirit or scope of the invention. Thus, it isintended that the present invention cover the modifications andvariations of this invention provided they come within the scope of theappended claims and their equivalents.

What is claimed is:
 1. A glass comprising, in mole percent:    58-62%SiO₂;    8-13% Al₂O₃;    6-12% B₂O₃;   0-7% MgO;    0-12% SrO;    0-16%CaO; and   2-9% BaO,

wherein MgO+CaO+BaO+SrO is greater than 14 to 20 percent, and whereinthe glass is substantially free of alkali metal, and wherein the glassis characterized by a liquidus temperature of 1150° C. or lower.
 2. Theglass according to claim 1, comprising 2-11% CaO.
 3. The glass accordingto claim 1, comprising 2-3.6% BaO.
 4. The glass according to claim 1,wherein the glass has a liquidus viscosity of 100,000 poise or greater.5. The glass according to claim 1, wherein MgO+CaO+BaO+SrO is 16 to 20percent.
 6. The glass according to claim 1, having a coefficient ofthermal expansion in the range of from about 35×10⁻⁷/° C. to about50×10⁻⁷/° C.
 7. The glass according to claim 1, comprising 0 to about 2mole percent of TiO₂, MnO, ZnO, Nb₂O₅, Ta₂O₅, ZrO₂, La₂O₃, Y₂O₃, P₂O₅,or a combination thereof.
 8. The glass according to claim 1, wherein theglass is in the form of a sheet.
 9. The glass according to claim 1,comprising 62 mole % SiO₂.
 10. The glass according to claim 1,comprising, in mole percent:   62% SiO₂; 11.1% Al₂O₃; 10.7% B₂O₃;  4.6%MgO;  3.6% SrO;  5.4% CaO; and  2.4% BaO.


11. The glass according to claim 1, comprising, in mole percent:   62%SiO₂; 10.3% Al₂O₃; 10.1% B₂O₃;  4.2% MgO;  2.9% SrO;  5.6% CaO; and 4.9% BaO.


12. The glass according to claim 1, comprising, in mole percent:   62%SiO₂; 10.8% Al₂O₃; 10.4% B₂O₃;  4.4% MgO;  3.3% SrO;  5.5% CaO; and 3.7% BaO.


13. A photovoltaic device comprising the glass according to claim 1.